A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700687



Internal ID15437339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:12299021..12311547hg38UCSC Ensembl
Innerchr17:12202338..12214864hg19UCSC Ensembl
Innerchr17:12143063..12155589hg18UCSC Ensembl
Innerchr17:12143063..12155589hg17UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3812527
hg1912527
hg1812527
hg1712527
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524704
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700687
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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